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    FDA Registration Active 🇺🇸 United States

    Validate Fibrinogen st Calibration Verification/Linearity Test Kit, product code 904st

    Reg #: 1226774 · FEI: 3003407015 · Expires 2025
    View on FDA
    Products
    1
    Proprietary Names
    4
    Establishment Types
    1
    Classifications
    1

    Registration Details

    Registration Name
    LGC Clinical Diagnostics, Inc.
    Registration Number
    1226774
    FEI Number
    3003407015
    Status
    Active
    Expiry Year
    2025
    Initial Importer
    No
    Address
    221 US Route 1
    City
    Cumberland Foreside
    State
    ME
    ZIP
    04110
    Country
    US

    Owner / Operator

    Firm Name
    LGC Clinical Diagnostics, Inc.
    Operator Number
    9041170
    Address
    37 Birch Street, --
    City
    Milford
    State
    MA
    Postal Code
    01757
    Country
    US

    Products

    Device Name Product Code
    Plasma, Fibrinogen Control GIL

    Proprietary Names

    Validate Fibrinogen st Calibration Verification/Linearity Test Kit, product code 904st Validate Fibrinogen il Calibration Verification/Linearity Test Kit, product code 904il Plasma, fibrinogen control Validate Fibrinogen se Calibration Verification/Linearity Test Kit, product code 904se

    Establishment Types

    Manufacture Medical Device